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Alleviating Structure Collapse of Polycrystalline LiNixCoyMn1-x-yO2 via Surface Co Enrichment.
Shang, Mingjie; Ren, Hengyu; Zhao, Wenguang; Li, Zijian; Fang, Jianjun; Chen, Hui; Fan, Wenguang; Pan, Feng; Zhao, Qinghe.
Afiliação
  • Shang M; School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
  • Ren H; School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
  • Zhao W; School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
  • Li Z; School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
  • Fang J; School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
  • Chen H; Qiantu Battery Technology Co., Ltd, Dongguan 523808, China.
  • Fan W; School of Materials and Environmental Engineering, Shenzhen Polytechnic University, 7098 Liuxian Boulevard, Shenzhen 518055, China.
  • Pan F; School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
  • Zhao Q; School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
ACS Nano ; 18(26): 16982-16993, 2024 Jul 02.
Article em En | MEDLINE | ID: mdl-38900971
ABSTRACT
The structure collapse issues have long restricted the application of polycrystalline LiNixCoyMn1-x-yO2 (NCM) at high voltages beyond 4.4 V vs Li/Li+. Herein, for LiNi0.55Co0.12Mn0.33O2 (P-NCM), rapid surface degradation is observed upon the first charge, along with serious particle fragmentation upon repeated cycles. To alleviate these issues, a surface Co enrichment strategy is proposed [i.e., Co-enriched NCM (C-NCM)], which promotes the in situ formation of a robust surface rock-salt (RS) layer upon charge, serving as a highly stable interface for effective Li+ migration. Benefiting from this stabilized surface RS layer, Li+ extraction occurs mainly through this surface RS layer, rather than along the grain boundaries (GBs), thus reducing the risk of GBs' cracking and even particle fragmentation upon cycles. Besides, O loss and TM (TM = Ni, Co, and Mn) dissolution are also effectively reduced with fewer side reactions. The C-NCM/graphite cell presents a highly reversible capacity of 205.1 mA h g-1 at 0.2 C and a high capacity retention of 86% after 500 cycles at 1 C (1 C = 200 mA g-1), which is among the best reported cell performances. This work provides a different path for alleviating particle fragmentation of NCM cathodes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Nano Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Nano Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China